ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.961-5981A>T

dbSNP: rs112213679
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001681001 SCV001896099 benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Natera, Inc. RCV001827578 SCV002090435 benign Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2017-04-20 no assertion criteria provided clinical testing

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